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CASE REPORT
Cornelia de Lange and Ehlers-Danlos: comorbidity of two rare syndromes
  1. Cora Cravero1,
  2. Vincent Guinchat1,
  3. Stéphane Barete2,
  4. Angèle Consoli1,3
  1. 1Department of Child and Adolescent Psychiatry, Reference Centre for Rare Psychiatric Diseases, AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Université Pierre et Marie Curie, Paris, France
  2. 2Unit of Dermatology, AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Université Pierre et Marie Curie, Paris, France
  3. 3INSERM U669, Maison de Solenn, Paris, France
  1. Correspondence to Dr Cora Cravero, cora.cravero{at}aphp.fr

Summary

We present a case of a young adult with both Cornelia de Lange syndrome and Ehlers-Danlos syndrome. The patient showed non-verbal autism, intellectual disability and severe/intractable self-harming behaviours that led to a life-threatening complication (ie, septicaemia). A significant reduction in the self-harming behaviours was attained in a multidisciplinary neurobehavioural inpatient unit after addressing all causes of somatic pains, managing pain using level II and III analgesics, stabilising the patient's mood, limiting the iatrogenic effects of multiple prescriptions and offering a specific psychoeducational approach.

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